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Linnankivi, Tarja
77
results:
Search for persons
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Format
Online (77)
Mediatypes
Articles (Online) (21)
OpenAccess-fulltext (56)
Languages
english (70)
finnish (2)
Sorted by: Relevance
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?
1
Epilepsies with onset during the first year of life: A pros..:
Jonsson, Henna
;
Gaily, Eija
;
Stjerna, Susanna
...
Epilepsia Open. 9 (2024) 4 - p. 1393-1405 , 2024
Link:
https://doi.org/10.1002/..
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2
Missense variants in ANO4 cause sporadic encephalopathic or..:
Yang, Fang
;
Begemann, Anais
;
Reichhart, Nadine
...
The American Journal of Human Genetics. 111 (2024) 6 - p. 1184-1205 , 2024
Link:
https://doi.org/10.1016/..
?
3
Corrigendum: Intrafamilial variability in SLC6A1-related ne..:
Kassabian, Benedetta
;
Fenger, Christina Dühring
;
Willems, Marjolaine
...
Frontiers in Neuroscience. 17 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
4
Clinical and electrophysiological features of SCN8A variant..:
Lyu, Hang
;
Boßelmann, Christian M.
;
Johannesen, Katrine M.
...
eBioMedicine. 98 (2023) - p. 104855 , 2023
Link:
https://doi.org/10.1016/..
?
5
Intrafamilial variability in SLC6A1-related neurodevelopmen..:
Kassabian, Benedetta
;
Fenger, Christina Dühring
;
Willems, Marjolaine
...
Frontiers in Neuroscience. 17 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
6
Networks of cortical activity in infants with epilepsy:
Auno, Sami
;
Jonsson, Henna
;
Linnankivi, Tarja
..
Brain Communications. 4 (2022) 6 - p. , 2022
Link:
https://doi.org/10.1093/..
?
7
Visual field defects after vigabatrin treatment during infa..:
Jonsson, Henna
;
Lehto, Mikko
;
Vanhatalo, Sampsa
..
Developmental Medicine & Child Neurology. 64 (2021) 5 - p. 641-648 , 2021
Link:
https://doi.org/10.1111/..
?
8
Exome sequencing reveals predominantly de novo variants in ..:
Järvelä, Irma
;
Määttä, Tuomo
;
Acharya, Anushree
...
Human Genetics. 140 (2021) 7 - p. 1011-1029 , 2021
Link:
https://doi.org/10.1007/..
?
9
Phenotypic and Imaging Spectrum Associated With WDR45:
Adang, Laura A.
;
Pizzino, Amy
;
Malhotra, Alka
...
Pediatric Neurology. 109 (2020) - p. 56-62 , 2020
Link:
https://doi.org/10.1016/..
?
10
The spectrum of intermediate SCN8A‐related epilepsy:
Johannesen, Katrine M.
;
Gardella, Elena
;
Encinas, Alejandra C.
...
Epilepsia. 60 (2019) 5 - p. 830-844 , 2019
Link:
https://doi.org/10.1111/..
?
11
Defining the phenotypic spectrum of SLC6A1 mutations:
Johannesen, Katrine M.
;
Gardella, Elena
;
Linnankivi, Tarja
...
Epilepsia. 59 (2018) 2 - p. 389-402 , 2018
Link:
https://doi.org/10.1111/..
?
12
De novo variants in neurodevelopmental disorders with epile..:
EuroEPINOMICS RES Consortium
;
Heyne, Henrike O.
;
Singh, Tarjinder
...
Nature Genetics. 50 (2018) 7 - p. 1048-1053 , 2018
Link:
https://doi.org/10.1038/..
?
13
De Novo Mutations in Synaptic Transmission Genes Including ..:
Appenzeller, Silke
;
Balling, Rudi
;
Barisic, Nina
...
The American Journal of Human Genetics. 100 (2017) 1 - p. 179 , 2017
Link:
https://doi.org/10.1016/..
?
14
De novo loss- or gain-of-function mutations in KCNA2 cause ..:
EuroEPINOMICS RES
;
Syrbe, Steffen
;
Hedrich, Ulrike B S
...
Nature Genetics. 47 (2015) 4 - p. 393-399 , 2015
Link:
https://doi.org/10.1038/..
?
15
Selenoprotein biosynthesis defect causes progressive enceph..:
Anttonen, Anna-Kaisa
;
Hilander, Taru
;
Linnankivi, Tarja
...
Neurology. 85 (2015) 4 - p. 306-315 , 2015
Link:
https://doi.org/10.1212/..
1-15